Canonical Allele Identifier: PA2827999058
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490366

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Phe2561Tyr
CA16038409
NM_001354901.2:c.7682T>A